The c.1A > C start codon mutation in CLN3 is associated with a protracted disease course

BACKGROUND: CLN3 disease is a disorder of lysosomal homeostasis predominantly affecting the retina and the brain. The severity of the underlying mutations in CLN3 particularly determines onset and course of neurological deterioration. Given the highly conserved start codon code among eukaryotic spec...

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Detalles Bibliográficos
Autores principales: Kuper, Willemijn F. E., van Alfen, Claudia, van Eck, Linda, de Man, Stella A., Willemsen, Marjolein H., van Gassen, Koen L. I., Losekoot, Monique, van Hasselt, Peter M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2020
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7052694/
https://www.ncbi.nlm.nih.gov/pubmed/32154056
http://dx.doi.org/10.1002/jmd2.12097

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7052694/
https://www.ncbi.nlm.nih.gov/pubmed/32154056
http://dx.doi.org/10.1002/jmd2.12097

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